dextroamphetamine sulfate

Generic: dextroamphetamine sulfate

Labeler: kvk-tech, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dextroamphetamine sulfate
Generic Name dextroamphetamine sulfate
Labeler kvk-tech, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dextroamphetamine sulfate 10 mg/1

Manufacturer
KVK-Tech, Inc.

Identifiers & Regulatory

Product NDC 10702-066
Product ID 10702-066_0f296f50-a802-d586-e063-6394a90a4888
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203548
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2015-11-23

Pharmacologic Class

Classes
central nervous system stimulant [epc] central nervous system stimulation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10702066
Hyphenated Format 10702-066

Supplemental Identifiers

RxCUI
884385 884386
UPC
0310702065017
UNII
JJ768O327N

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name dextroamphetamine sulfate (source: ndc)
Generic Name dextroamphetamine sulfate (source: ndc)
Application Number ANDA203548 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (10702-066-01)
  • 30 TABLET in 1 BOTTLE (10702-066-03)
  • 60 TABLET in 1 BOTTLE (10702-066-06)
source: ndc

Packages (3)

10702-066-01 100 TABLET in 1 BOTTLE (10702-066-01) 10702-066-03 30 TABLET in 1 BOTTLE (10702-066-03) 10702-066-06 60 TABLET in 1 BOTTLE (10702-066-06)

Ingredients (1)

dextroamphetamine sulfate (10 mg/1)

Linked Drug Pages (1)

Dextroamphetamine Sulfate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0f296f50-a802-d586-e063-6394a90a4888", "openfda": {"upc": ["0310702065017"], "unii": ["JJ768O327N"], "rxcui": ["884385", "884386"], "spl_set_id": ["863d66fe-9c38-463a-afa1-552647494c5a"], "manufacturer_name": ["KVK-Tech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-066-01)", "package_ndc": "10702-066-01", "marketing_start_date": "20151123"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (10702-066-03)", "package_ndc": "10702-066-03", "marketing_start_date": "20151123"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (10702-066-06)", "package_ndc": "10702-066-06", "marketing_start_date": "20151123"}], "brand_name": "Dextroamphetamine Sulfate", "product_id": "10702-066_0f296f50-a802-d586-e063-6394a90a4888", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "10702-066", "dea_schedule": "CII", "generic_name": "Dextroamphetamine Sulfate", "labeler_name": "KVK-Tech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextroamphetamine Sulfate", "active_ingredients": [{"name": "DEXTROAMPHETAMINE SULFATE", "strength": "10 mg/1"}], "application_number": "ANDA203548", "marketing_category": "ANDA", "marketing_start_date": "20151123", "listing_expiration_date": "20261231"}